SNX15

SNX15
Identifiers
Aliases	SNX15, HSAF001435, sorting nexin 15
External IDs	OMIM: 605964; MGI: 1916274; HomoloGene: 12294; GeneCards: SNX15; OMA:SNX15 - orthologs
Gene location (Mouse)
Chr.	Chromosome 19 (mouse)
End	6,178,334 bp
RNA expression pattern
	Top expressed in
	bone marrow cells; ; prefrontal cortex; ; cerebellar hemisphere; ; monocyte; ; skeletal muscle tissue; ; gastrocnemius muscle; ; popliteal artery; ; right coronary artery; ; Brodmann area 9; ; amygdala;
	Top expressed in
	blood; ; neural layer of retina; ; superior frontal gyrus; ; fetal liver hematopoietic progenitor cell; ; islet of Langerhans; ; yolk sac; ; lip; ; gastric mucosa; ; primary visual cortex; ; epithelium of stomach;
	More reference expression data
	n/a
Gene ontology
Molecular function	protein binding; phosphatidylinositol binding; lipid binding;
Cellular component	nucleolus; cytoplasmic vesicle membrane; membrane; cytoplasmic vesicle; cytoplasm; cytosol;
Biological process	protein transport; signal transduction; intracellular protein transport;
	Sources:Amigo / QuickGO
Orthologs
	29907
	69024
	n/a
	ENSMUSG00000024787
	Q9NRS6
	Q91WE1
	NM_147777; NM_013306
	NM_026912
	NP_037438; NP_680086
	NP_081188
	Wikidata
View/Edit Human	View/Edit Mouse

Sorting nexin-15 is a protein that in humans is encoded by the SNX15 gene.^[4]^[5]

This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. Overexpression of this gene results in a decrease in the processing of insulin and hepatocyte growth factor receptors to their mature subunits. This decrease is caused by the mislocalization of furin, the endoprotease responsible for cleavage of insulin and hepatocyte growth factor receptors. This protein is involved in endosomal trafficking from the plasma membranee to recycling endosomes or the trans-Golgi network. This gene encodes two transcript variants encoding distinct isoforms.^[5]

References

^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000024787 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Barr VA, Phillips SA, Taylor SI, Haft CR (Mar 2001). "Overexpression of a novel sorting nexin, SNX15, affects endosome morphology and protein trafficking". Traffic. 1 (11): 904–16. doi:10.1034/j.1600-0854.2000.011109.x. PMID 11208079. S2CID 31092568.
^ ^a ^b "Entrez Gene: SNX15 sorting nexin 15".

Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
Guru SC, Agarwal SK, Manickam P, et al. (1997). "A transcript map for the 2.8-Mb region containing the multiple endocrine neoplasia type 1 locus". Genome Res. 7 (7): 725–35. doi:10.1101/gr.7.7.725. PMC 310681. PMID 9253601.
Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
Phillips SA, Barr VA, Haft DH, et al. (2001). "Identification and characterization of SNX15, a novel sorting nexin involved in protein trafficking". J. Biol. Chem. 276 (7): 5074–84. doi:10.1074/jbc.M004671200. PMID 11085978.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. Bibcode:2005Natur.437.1173R. doi:10.1038/nature04209. PMID 16189514. S2CID 4427026.

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[refGRCm38Ensembl-1] GRCm38: Ensembl release 89: ENSMUSG00000024787 – Ensembl, May 2017

[2] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[3] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid11208079-4] Barr VA, Phillips SA, Taylor SI, Haft CR (Mar 2001). "Overexpression of a novel sorting nexin, SNX15, affects endosome morphology and protein trafficking". Traffic. 1 (11): 904–16. doi:10.1034/j.1600-0854.2000.011109.x. PMID 11208079. S2CID 31092568.

[entrez-5] "Entrez Gene: SNX15 sorting nexin 15".

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v t e Sorting nexins
SNX-BAR	SNX1 SNX2 SNX4 SNX5 SNX6 SNX7 SNX8 SNX9 SNX18 SNX30 SNX32 SNX33
SNX-PX	SNX3 SNX10 SNX11 SNX12 SNX16 SNX20 SNX21 SNX22 SNX24 SNX29
SNX-Other	SNX13 SNX14 SNX15 SNX17 SNX19 SNX23 SNX25 SNX26 SNX27 SNX28 SNX31
Related articles	PX domain BAR domain Retromer

SNX15

References

Further reading